FDA Recalls, Food, Drug & Medical Device Alerts - Page 33 of 46

Latest food, drug, and medical device recalls issued by the U.S. Food and Drug Administration. Class I, II, and III recall classifications, affected products, and consumer guidance.

Showing 1,601–1,650 of 2,262 FDA recalls. Browse by month →

FDA Recalls

Recall of GE Healthcare's Omnipaque Injection Due to Particulate Matter

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FDA Recalls

Recall of Vancomycin HCL Injection by Fagron Compounding Services

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FDA Recalls

Teva Pharmaceuticals Recalls Isotretinoin Capsules Over Potency Concerns

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FDA Recalls

Recall of Sodium Chloride Injection by Fresenius Kabi

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FDA Recalls

Recall of 0.9% Sodium Chloride Injection Due to Sterility Concerns

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FDA Recalls

FDA Recall of Norepinephrine Bitartrate Injection by Fagron Compounding Services

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FDA Recalls

FDA Recall of Artificial Tears Eye Drops Due to Sterility Concerns

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FDA Recalls

Xanax XR Tablets Recall Over Failed Dissolution Specifications

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FDA Recalls

Recall of Fresenius Kabi 0.9% Sodium Chloride Injection

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FDA Recalls

Recall of Dextrose Injection by Fresenius Kabi USA

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FDA Recalls

FDA Recall of Fresenius Kabi Dextrose Injection

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FDA Recalls

FDA Recall of Clonidine Transdermal System Due to Manufacturing Issue

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FDA Recalls

Recall of Fresenius Kabi 5% Dextrose Injection Due to Sterility Concerns

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FDA Recalls

FDA Recall of Sodium Chloride Injection Due to Sterility Concerns

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FDA Recalls high

FDA Recall of Vancomycin HCI Injection by Fagron Compounding Services

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FDA Recalls

Recall of Clonidine Transdermal System Due to Manufacturing Issue

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FDA Recalls

FDA Recall of Fresenius Kabi's Sodium Chloride Injection

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FDA Recalls

Recall of Fresenius Kabi Sodium Chloride Injection

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FDA Recalls

Fresenius Kabi Sodium Chloride Injection Recall

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FDA Recalls

Clonidine Transdermal System Recall Over Manufacturing Issue

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FDA Recalls

FDA Recall of Fresenius Kabi Sodium Chloride Injection

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FDA Recalls

Fagron Compounding Services Issues Recall for Vancomycin HCI Injection

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FDA Recalls

Philips Azurion 7 B12 Recall for X-ray Imaging Issues

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FDA Recalls

FDA Recall of Synthes 2.4 VOLT(TM) TAP CORTEX SCREW

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FDA Recalls

Recall of Philips Allura Xper FD10C Systems

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FDA Recalls high

Recall of Medline Anterior Hip Pack Due to Safety Issue

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FDA Recalls high

FDA Recall of Medtronic MiniMed 700G Insulin Pump for Delivery Issues

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FDA Recalls

Recall of Paradise Catheter by ReCor Medical Inc.

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FDA Recalls

FDA Announces Recall of Philips Vue Motion V12 Medical Device

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FDA Recalls

Philips Azurion 7 M20 Recall for X-ray Imaging Issues

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FDA Recalls

Philips ALLURA Xper FD20 Recall for Imaging Issues

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FDA Recalls

Burlington Medical BAT Coverage Recall

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FDA Recalls

FDA Recall of da Vinci S, Si Tenaculum Forceps Instrument

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FDA Recalls

Burlington Medical Kilt Recall Over Attenuation Degradation

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FDA Recalls

FDA Recall of Philips Allura Xper FD20/20 Systems

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FDA Recalls

Recall of Philips Allura Xper FD20/15 Medical Device

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FDA Recalls high

FDA Recall of Philips Respironics Trilogy Evo Ventilator

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FDA Recalls

Burlington Medical Caps Recall

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FDA Recalls high

FDA Recall of Medline Kits Containing Olympus Biopsy Valves

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FDA Recalls

Stryker CHROMOPHARE Softlit Ring Surgical Light System Recall

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FDA Recalls

Recall of Philips ALLURA Xper FD10 OR Table for Imaging Issues

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FDA Recalls

Burlington Medical Thyroid Shield Recall

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FDA Recalls

Recall of eTRAX Needle System Starter Kit by Civco Medical Instruments

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FDA Recalls

Recall of Philips ALLURA Xper FD10/10 Medical Devices

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FDA Recalls high

Recall of Medtronic MiniMed 770G Insulin Pumps for Delivery Issues

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FDA Recalls

Recall of da Vinci S, Si Double Fenestrated Grasper Instrument

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FDA Recalls

Medline Industries Recalls Sterile Radiology Procedure Kits

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FDA Recalls

FDA Recall of Finesse BTK Multicath by SUMMA THERAPEUTICS

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FDA Recalls

Recall of Olympus SOLTIVE Pro Laser System Due to Power Supply Defect

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FDA Recalls high

Medline Convenience Kits Recall Over Biopsy Valve Issue

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